Olefin epoxidation process, a catalyst for use in the process, a carrier for use in preparing the catalyst, and a process for preparing the carrier

ABSTRACT

A process is provided for preparing a carrier which process comprises incorporating into the carrier at any stage of the carrier preparation a strength-enhancing additive. Also provided is the resultant carrier having incorporated therein a strength-enhancing additive and a catalyst comprising the carrier. Also provided is a process for the epoxidation of an olefin employing the catalyst. Also provided is a method of using the olefin oxide so produced for making a 1,2-diol, a 1,2-diol ether or an alkanolamine.

The present application is a continuation of U.S. application Ser. No.11/215,267 filed Aug. 30, 2005 now U.S. Pat. No. 7,560,411, the entiredisclosure of which is hereby incorporated by reference.

This application claims the benefit of U.S. Provisional Application No.60/606,193 filed Sep. 1, 2004, the entire disclosure of which is herebyincorporated by reference.

FIELD OF THE INVENTION

The present invention relates to a process for the production of anolefin oxide, a 1,2-diol, a 1,2-diol ether, or an alkanolamine. Thepresent invention also relates to a catalyst for use in the process forthe production of an olefin oxide and a carrier for use in preparing thecatalyst. The present invention also relates to a process for preparingthe carrier.

BACKGROUND OF THE INVENTION

In olefin epoxidation, a feed containing an olefin and an oxygen sourceis contacted with a catalyst under epoxidation conditions. The olefin isreacted with oxygen to form an olefin oxide. A product mix results thatcontains olefin oxide and typically unreacted feed and combustionproducts, such as carbon dioxide.

The catalyst comprises silver, usually with one or more additionalelements deposited therewith, on a carrier, typically an alpha-aluminacarrier. The olefin oxide may be reacted with water to form a 1,2-diol,with an alcohol to form a 1,2-diol ether, or with an amine to form analkanolamine. Thus, 1,2-diols, 1,2-diol ethers, and alkanolamines may beproduced in a multi-step process initially comprising olefin epoxidationand then the conversion of the formed olefin oxide with water, analcohol, or an amine.

The performance of the silver containing catalyst may be assessed on thebasis of selectivity, activity, and stability of operation in the olefinepoxidation. The selectivity is the molar fraction of the convertedolefin yielding the desired olefin oxide. Stability refers to how theselectivity and/or activity of the process changes during the time acharge of catalyst is being used, i.e., as more olefin oxide isproduced.

Various approaches to improving the performance of the silver catalysts,including improvements in selectivity, activity, and stability, havebeen investigated. For example, modern silver-based catalysts maycomprise, in addition to silver, one or more high-selectivity dopants,such as components comprising rhenium, tungsten, chromium, ormolybdenum. High-selectivity catalysts are disclosed, for example, inU.S. Pat. No. 4,761,394 and U.S. Pat. No. 4,766,105. U.S. Pat. No.4,766,105 and U.S. Pat. No. 4,761,394 disclose that rhenium may beemployed as a further component in the silver containing catalyst withthe effect that the initial, peak selectivity of the olefin epoxidationis increased.

Depending upon the catalyst used and the parameters of the olefinepoxidation process, the time required to reach the initial, peakselectivity, that is the highest selectivity reached in the initialstage of the process, may vary. For example, the initial, peakselectivity of a process may be achieved after only 1 or 2 days ofoperation or may be achieved after as much as, for example, 1 month ofoperation. EP-A-352850 also teaches that the then newly developedcatalysts, comprising silver supported on alumina carrier, promoted withalkali metal and rhenium components have a very high selectivity.

As another example of an approach to improving the performance of thesilver catalysts, fluorine has been incorporated into carriers used toprepare epoxidation catalysts, with an intention that the resultantfluoride-mineralized carriers will have morphological propertiesconducive to improved catalyst performance. The crush strength orattrition resistance of such fluoride-mineralized carriers, however, canoften be inherently lower than desirable. While various additives, oftenreferred to as binders, have been used to improve the crush strength orattrition resistance of carriers, traditional binders typically must besubjected to a high temperature treatment to activate their bindingproperties. Often, the high temperature treatment involves temperaturesin excess of 1,200° C., even in excess 1,300° C. The use of suchtraditional binders with fluoride-mineralized carriers may not bedesirable, as the morphology of the fluoride-mineralized carrier may bedetrimentally affected if the carrier is exposed to such hightemperatures.

Thus, notwithstanding the improvements already achieved, there is adesire to improve the performance of olefin epoxidation catalysts and,in particular, to increase the crush strength or attrition resistance offluoride-mineralized carriers without detrimentally affecting themorphology of such carriers.

SUMMARY OF THE INVENTION

The present invention relates to a process for the production of anolefin oxide, a 1,2-diol, a 1,2-diol ether, or an alkanolamine. Thepresent invention also relates to a catalyst for use in the process forthe production of olefin oxide and a carrier for use in preparing thecatalyst. The present invention also relates to a process for preparingthe carrier.

The invention provides a process for increasing the crush strength orattrition resistance of a fluoride-mineralized carrier comprisingincorporating into the fluoride-mineralized carrier a strength-enhancingadditive. In preferred embodiments, amongst others, thestrength-enhancing additive is selected from the group consisting of azirconium species, a lanthanide Group species, a Group II metal species,an inorganic glass, and mixtures thereof.

The invention also provides a fluoride-mineralized carrier havingincorporated therein a strength-enhancing additive. In preferredembodiments, amongst others, the fluoride-mineralized carrier comprisesalpha-alumina.

The invention also provides a process for preparing afluoride-mineralized carrier, which process comprises incorporating intothe carrier at any stage of the carrier preparation a strength-enhancingadditive.

The invention also provides a catalyst for the epoxidation of an olefincomprising a silver component deposited on a fluoride-mineralizedcarrier, wherein the fluoride-mineralized carrier has incorporatedtherein a strength-enhancing additive. In preferred embodiments, amongstothers, the catalyst additionally comprises a high-selectivity dopant.In preferred embodiments, amongst others, the catalyst additionallycomprises a rhenium component or a rhenium component and rheniumco-promoter. In preferred embodiments, amongst others, the catalystadditionally comprises a Group IA metal component.

The invention also provides a process for the epoxidation of an olefincomprising the steps of contacting a feed comprising an olefin andoxygen with a catalyst comprising a silver component deposited on afluoride-mineralized carrier and producing a product mix comprising anolefin oxide, wherein the fluoride-mineralized carrier has incorporatedtherein a strength-enhancing additive. The fluoride-mineralized carriermay have, and preferably does have, a particulate matrix having amorphology characterizable as lamellar or platelet-type, which terms areused interchangeably. As such, particles having in at least onedirection a size greater than 0.1 micrometers have at least onesubstantially flat major surface. Such particles may have two or moreflat major surfaces. In alternative embodiments of this invention, thecarrier has said platelet-type structure and has been prepared by amethod other than the fluoride-mineralization methods described herein.

In preferred embodiments, amongst others, the catalyst additionallycomprises a high-selectivity dopant. In preferred embodiments, amongstothers, the catalyst additionally comprises a rhenium component or arhenium component and a rhenium co-promoter. In preferred embodiments,amongst others, the catalyst additionally comprises a Group IA metalcomponent. In preferred embodiments, amongst others, the processexhibits a selectivity to the olefin oxide greater than 85%, preferablygreater than 87%, more preferably greater than about 89%, and even morepreferably greater than about 90% and frequently as much as about 92%.

The invention also provides a process for the production of a 1,2-diol,a 1,2-diol ether, or an alkanolamine comprising converting an olefinoxide into the 1,2-diol, the 1,2-diol ether, or the alkanolamine,wherein the olefin oxide has been obtained by a process for theepoxidation of an olefin comprising reacting the olefin with oxygen inaccordance with this invention.

It is envisioned that catalysts comprising the carrier of this inventionand an amount of an appropriate catalytic species, frequently a metallicspecies such as silver, molybdenum, nickel, and tungsten, or compoundsthereof, may advantageously be employed in other conversion processes.

The features and advantages of the present invention will be readilyapparent to those skilled in the art upon reading the description of theinvention that follows.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a process for the production of anolefin oxide, a 1,2-diol, a 1,2-diol ether, or an alkanolamine. Thepresent invention also relates to a catalyst for use in the process forthe production of an olefin oxide and a carrier for use in preparing thecatalyst. The present invention also relates to a process for preparingthe carrier.

The invention provides a process for increasing the crush strength orattrition resistance of a fluoride-mineralized carrier in which astrength-enhancing additive is incorporated into thefluoride-mineralized carrier. The invention also provides a catalyst forthe epoxidation of an olefin comprising a silver component deposited ona fluoride-mineralized carrier, wherein the fluoride-mineralized carrierhas incorporated therein a strength-enhancing additive. The inventionalso provides a process for the epoxidation of an olefin comprising thesteps of contacting a feed comprising an olefin and oxygen with acatalyst comprising a silver component deposited on afluoride-mineralized carrier and producing a product mix comprising anolefin oxide, wherein the fluoride-mineralized carrier has incorporatedtherein a strength-enhancing additive.

Fluoride-Mineralized Carrier

Fluoride-mineralized carriers are obtained by the incorporation offluorine into the carrier. For purposes of the present invention,fluoride-mineralized carriers are obtained by combining alpha-alumina oralpha-alumina precursor(s) with a fluorine-containing species that iscapable of liberating fluoride, typically as hydrogen fluoride, when thecombination is calcined, and calcining the combination. Prior tocalcining, the combination may be formed into formed bodies, for exampleby extrusion or spraying. Preferably, calcination is conducted at lessthan about 1,200° C., more preferably at less than about 1,100° C.Preferably, calcination is conducted at greater than about 900° C., morepreferably at greater than about 1,000° C. If the temperature issufficiently in excess of 1,200° C., the amount of fluoride liberatedmay be excessive and the morphology of the carrier may be detrimentallyaffected.

The manner by which the fluorine-containing species is introduced intothe carrier is not limited, and those methods known in the art forincorporating a fluorine-containing species into a carrier, and thosefluoride-mineralized carriers obtained therefrom, may be used for thepresent invention. For example, U.S. Pat. No. 3,950,507 and U.S. Pat.No. 4,379,134 disclose methods for preparing fluoride-mineralizedcarriers and are hereby incorporated by reference.

As indicated hereinbefore, the fluoride-mineralized carriers may have,and preferably do have, a particulate matrix having a morphologycharacterizable as lamellar or platelet-type, which terms are usedinterchangeably. As such, particles having in at least one direction asize greater than about 0.1 micrometers have at least one substantiallyflat major surface. Such particles may have two or more flat majorsurfaces. In alternative embodiments of this invention, carriers may beused which have said platelet-type structure and which have beenprepared by a method other than the fluoride-mineralization methodsdescribed herein.

A suitable procedure for incorporating a fluorine-containing speciesinto a carrier involves adding a fluorine-containing species toalpha-alumina or an alpha-alumina precursor(s). The alpha-aluminaprecursors mentioned herein are those species capable of being convertedto alpha-alumina upon calcination. The alpha-alumina precursors includehydrated aluminas, such as boehmite, pseudoboehmite, and gibbsite, aswell as transition aluminas, such as the chi, kappa, gamma, delta,theta, and eta aluminas.

If a hydrated alumina is used, a fluorine-containing species suitablymay be added to the hydrated alumina with the combination then made intoformed bodies, such as by extrusion or spraying. The hydrated alumina isthen converted to alpha-alumina by calcining the formed bodies.Preferably, the calcination is conducted at less than about 1,200° C.During the calcination, fluoride is liberated. Similarly, afluorine-containing species suitably may be added to a transitionalumina, such as gamma alumina, or to a combination of transitionalumina and hydrated alumina. The combination is made into formed bodiesand calcined, as before.

In another suitable method, a fluorine-containing species may be addedto formed bodies of alpha-alumina or an alpha-alumina precursor(s) ormixtures thereof. The formed bodies are then subjected to calcination.In another suitable method, the fluorine-containing species may be addedto the carrier after calcination, i.e., after formation ofalpha-alumina. In such a method, the fluorine-containing species may beconveniently incorporated in the same manner as silver and any otherpromoters, e.g., by impregnation, typically vacuum impregnation.

As previously explained, calcination is preferably conducted at lessthan about 1,200° C. The present invention, however, is independent ofthe manner by which calcination is conducted. Thus, variations incalcining known in the art, such as holding at one temperature for acertain period of time and then raising the temperature to a secondtemperature over the course of a second period of time, are contemplatedby the present invention.

The addition of the fluorine-containing species may be by any knownmethod. In one such suitable method, the alpha-alumina or alpha-aluminaprecursor(s) is treated with a solution containing a fluorine-containingspecies. The combination is co-mulled and extruded. Similarly, formedbodies may be subjected to vacuum impregnation with a solutioncontaining a fluorine-containing species. Any combination of solvent andfluorine-containing species that results in the presence of fluorideions in solution may be used in accordance with such a method.

Fluorine-containing species that may be used in accordance with thisinvention are those species that when incorporated into a carrier inaccordance with this invention are capable of liberating fluoride,typically in the form of hydrogen fluoride, when calcined, preferably atless than about 1,200° C. Preferred fluorine-containing species arecapable of liberating fluoride when calcining is conducted at atemperature of from about 900° C. to about 1,200° C. Suchfluorine-containing species known in the art may be used in accordancewith this invention. Suitable fluorine-containing species includeorganic and inorganic species. Suitable fluorine-containing speciesinclude ionic, covalent, and polar covalent compounds. Suitablefluorine-containing species include F₂, aluminum trifluoride, ammoniumfluoride, hydrofluoric acid, and dichlorodifluoromethane.

Typically, the amount of fluorine-containing species added to thecarrier is at least about 0.1 percent by weight and typically no greaterthan about 5 percent by weight, calculated as the weight of elementalfluorine used relative to the weight of the carrier material to whichthe fluorine-containing species is being incorporated. Frequently, thefluorine-containing species is used in an amount from about 0.2 to about3 percent by weight. More frequently, the fluorine-containing species isused in an amount from about 0.25 to about 2.5 percent by weight. Theseamounts refer to the amount of the species as initially added and do notnecessarily reflect the amount that may ultimately be present in thefinished carrier.

An advantage of the present invention is that the fluoride-mineralizedcarriers, or carriers having a particulate matrix having a lamellar orplatelet-type morphology, have incorporated therein an additive thatserves to increase the crush strength or attrition resistance of thecarrier. Strength-enhancing additives are those species that whenincorporated into the carrier result in an increase in the crushstrength or improvement in the attrition resistance of the carrier.Suitably, the strength-enhancing additives are easily incorporated intothe alumina crystal structure of the carrier, for example into thealumina crystal structure of a fluoride-mineralized carrier, bycalcination at temperatures less than about 1,200° C., more preferablyat less than about 1,100° C. Frequently, the strength-enhancingadditives are easily incorporated into the alumina crystal structure ofthe carrier by calcination at temperatures greater than about 900° C.,more frequently at greater than about 1,000° C. Preferably, thestrength-enhancing additive is capable of forming fluoride species,typically having a relatively low volatility so as to enhance theirinteraction with the carrier leading to the strength-enhancing effect.Strength-enhancing additives may be selected from the group consistingof a zirconium species, a lanthanide Group species, a Group II metalspecies, an inorganic glass, and mixtures thereof.

The specific form in which the strength-enhancing additive exists priorto being incorporated into the carrier is not limited. Thus, zirconiumspecies, a lanthanide Group species, and Group II metal species includesany specific element as such and compounds of the element. Illustrativestrength-enhancing additives include ammonium fluorozirconate, calciumzirconate, zirconium acetate, zirconium acetylacetonate, zirconiumcarbonate, zirconium fluoride, zirconium oxynitrate, zirconium silicate,lanthanum carbonate, lanthanum fluoride, lanthanum nitrate, lanthanumoxalate, lanthanum oxide, cerium carbonate, cerium fluoride, ceriumnitrate, cerium oxalate, cerium oxide, magnesium acetate, magnesiumcarbonate, magnesium fluoride, magnesium nitrate, magnesium oxalate,magnesium oxide, calcium acetate, calcium carbonate, calcium fluoride,calcium nitrate, calcium oxalate, and calcium oxide.

Preferably, the inorganic glass has a melting temperature that is atmost the temperature at which the calcination is carried out. Forexample, the inorganic glass may have a melting temperature that isbelow 1,200° c. Melting temperature of the inorganic glass is understoodto mean the temperature at which the ingredients of the inorganic glasswould be heated during glass manufacture to obtain a fluid. Typicalinorganic glass compositions may include the elements silicon, boron,aluminum, or lead in combination with many other elements, such asalkali and alkaline earth metals. These elements are typically employedas their oxides. Illustrative inorganic glass compositions that may beused for purposes of the present invention include, among many others,the following: Na₂O.SiO₂+Na₂O.2SiO₂, Na₂O.2SiO₂+SiO₂ (quartz),K₂O.SiO₂+K₂O.2SiO₂, K₂O.2SiO₂+K₂O.4SiO₂, PbO, 2PbO.SiO₂+PbO.SiO₂,Na₂O.SiO₂+Na₂O.2SiO₂+2Na₂O.CaO.3SiO₂,K₂O.2SiO₂+K₂O.2CaO.9SiO₂+K₂O.4SiO₂, Na₂O.4B₂O₃+SiO₂, andNa₂O.2B₂O₃+Na₂O.SiO₂.

Within these limitations, the manner by which the strength-enhancingadditive is incorporated into the carrier is not generally limited.Similarly, the point in the process for preparing the carrier when thestrength-enhancing additive is incorporated is not generally limited.Indeed, it is expected that, depending on the specificstrength-enhancing additive or combination thereof used as well as theamount of the strength-enhancing additive used, those methods used toincorporate fluorine-containing species into the carrier as well asother methods may be suitably used to incorporate the strength-enhancingadditive. For example, in one such suitable method, the alpha-alumina oralpha-alumina precursor(s) is combined with a strength-enhancingadditive, such as calcium acetate. The strength-enhancing additive maybe used in the form of a composition comprising the strength-enhancingadditive, for example as a solution or as a dispersion in a diluent,suitably an aqueous diluent or, less preferred, an organic diluent. Thestrength-enhancing additive may be added simultaneously with thefluorine-containing species; however, the fluorine-containing speciesmay have been added previously or may be added subsequently. After thealpha-alumina or alpha-alumina precursor(s) is combined with thestrength-enhancing additive, the combination may be co-mulled and madeinto formed bodies and subsequently calcined. Similarly, an extrudate orother formed bodies may be combined with the strength-enhancingadditive, for example by subjecting the formed bodies to impregnation orvacuum impregnation with a solution or emulsion containing thestrength-enhancing additive, and subsequently calcined. When inorganicglass is used as the strength-enhancing additive, ground inorganic glassor the individual components of the desired inorganic glass may becombined with alpha-alumina or alpha-alumina precursor(s), with thecombination then being heated and made into formed bodies. The inorganicglass may be introduced in other manners. For example, in certainembodiments, the individual components of the inorganic glass may beintroduced as a solution in a solvent.

As indicated above, the present invention does not contemplate that thestrength-enhancing additive must be incorporated into the carriersimultaneously with the fluorine-containing species. The presentinvention contemplates that the strength-enhancing additive may beincorporated simultaneously, before, or after the fluorine-containingspecies. Suitable methods to incorporate the strength-enhancing additiveas well as suitable points during the process for preparing the carrierwhen the strength-enhancing additive is incorporated may be selected onthe basis of routine experimentation.

For purposes of the present invention, a strength-enhancing additivemay, for example, suitably be added to hydrated alumina, such asboehmite, with the combination then made into formed bodies andcalcined, as before. Similarly, a strength-enhancing additive maysuitably be added to a transition alumina, such as gamma alumina, or toa combination of transition alumina and hydrated alumina. Thecombination is made into formed bodies, for example by extrusion orspraying, and calcined, as before. In another suitable method, astrength-enhancing additive may be added to formed bodies ofalpha-alumina or an alpha-alumina precursor(s) or mixtures thereof. Theformed bodies are then subjected to calcination. In another suitablemethod, the strength-enhancing additive may be added to a carrier havinga particulate matrix having a lamellar or platelet-type morphology,i.e., after formation of alpha-alumina, and calcined. In such a method,the strength-enhancing additive may be conveniently incorporated in thesame manner as silver and any other promoters, e.g., by impregnation,typically vacuum impregnation.

The determination of an appropriate strength-enhancing amount of anyspecific strength-enhancing additive or combination ofstrength-enhancing additives for use in this invention is a matter ofroutine experimentation. Suitably, it is desirable to conductrange-finding experiments to determine the strength-enhancing amountrange for any specific strength-enhancing additive or combination ofadditives. A fluoride-mineralized carrier, or a carrier having aparticulate matrix having a lamellar or platelet-type morphology,containing no strength-enhancing additive is desirably prepared toprovide a basis of comparison. Any lower or upper concentration limitfor a specific strength-enhancing additive or combination thereof maythereafter be determined by preparing a series of carriers containingsuccessively larger amounts of the strength-enhancing additive orcombination thereof. The experiments will typically be continued untilthe measured crush strength or attrition resistance of the last carrieris inferior to that of the preceding carrier. The specific response ofany strength-enhancing additive or combination thereof may be furtherrefined, if desired, by conducting additional experiments withintermediate amounts of the strength-enhancing additive or combinationthereof.

While not being limited, it is expected that, typically, thestrength-enhancing amount of strength-enhancing additive will forzirconium species be at least about 0.1 percent by weight, frequently atleast about 0.2 percent by weight, more frequently at least about 0.5percent by weight, even more frequently at least about 1 percent byweight, and no greater than about 5 percent by weight, frequently nogreater than about 4 percent by weight, calculated as the weight of theelement zirconium used relative to the total weight of the carrier.While not being limited, it is expected that, typically, thestrength-enhancing amount of strength-enhancing additive will forlanthanide Group species be at least about 0.1 percent by weight,frequently at least about 0.2 percent by weight, more frequently atleast about 0.5 percent by weight, even more frequently at least about 1percent by weight, and no greater than about 5 percent by weight,frequently no greater than about 4 percent by weight, calculated as theweight of the lanthanide Group element used relative to the total weightof the carrier. While not being limited, it is expected that, typically,the strength-enhancing amount of strength-enhancing additive will forGroup II metal species be at least about 0.1 percent by weight,frequently 0.2 percent by weight, more frequently at least about 0.5percent by weight, even more frequently at least about 1 percent byweight, and no greater than about 5 percent by weight, frequently nogreater than about 4 percent by weight, calculated as the weight of theGroup II metal element used relative to the total weight of the carrier.While not being limited, it is expected that, typically, thestrength-enhancing amount of strength-enhancing additive will forinorganic glass be at least about 0.1 percent by weight, frequently atleast about 0.2 percent by weight, more frequently at least about 0.5percent by weight, even more frequently at least about 1 percent byweight, and no greater than about 5 percent by weight, frequently nogreater than about 4 percent by weight, calculated as the weight ofinorganic glass used relative to the total weight of the carrier. Theseamounts refer to the amount of the additive as initially added and donot necessarily reflect the amount that may ultimately be present in thefinished carrier.

For purposes of the present invention, the crush strength of a carrieror the attrition resistance of a carrier can be measured in a number ofways. A suitable way to measure crush strength is using ASTM D6175-03. Asuitable way to measure attrition resistance is using ASTM D4058-96. Byuse of these ASTM methods or other methods for testing crush strength orattrition resistance, a carrier having incorporated therein a certainamount of a strength-enhancing additive may be compared to othercarriers having a different strength-enhancing additive or a differentamount of the same strength-enhancing additive. Comparisons may also bemade to a comparable carrier that does not have incorporated therein astrength-enhancing additive. Thus, a carrier having incorporated thereina strength-enhancing amount of a strength-enhancing additive can beobtained. In certain embodiments, it is desirable to employ a strengthenhancing additive in amounts sufficient to achieve a carrier having apractical crush strength or practical attrition resistance for use inthe commercial production of olefin oxide. Suitably, thefluoride-mineralized carrier or the carrier having the lamellar orplatelet-type morphology has a crush strength of at least about 0.4pound-force per millimeter (lbf/mm) (approximately 1.8 N/mm), preferablyat least about 2 N/mm, more preferably at least about 3.5 N/mm, evenmore preferably at least about 5 N/mm and frequently as much as about 40N/mm, more frequently as much as about 25 N/mm, even more frequently asmuch as about 15 N/mm. Such crush strengths are measured in accordancewith ASTM D6175-03, wherein the test sample is tested as such after itspreparation, that is with elimination of Step 7.2 of said method, whichrepresents a step of drying the test sample. For this crush strengthtest method, the crush strength of a formed carrier is typicallymeasured as the crush strength of hollow cylindrical particles of 8.8 mmexternal diameter, 3.5 mm internal diameter, and 8 mm length.

Attrition resistance, as used herein, is measured in accordance withASTM D4058-96, wherein the test sample is tested as such after itspreparation, that is with elimination of Step 6.4 of the said method,which represents a step of drying the test sample. Preferably, thefluoride-mineralized carrier or the carrier having the lamellar orplatelet-type morphology exhibits, when in shaped form, in particular inthe form of hollow cylindrical particles of 8.8 mm external diameter,3.5 mm internal diameter and 8 mm length, attrition of at most 50percent, more preferably at most 40 percent, in particular at most 30percent. Frequently, the attrition may be at least 10 percent, inparticular at least 15%, more in particular at least 20 percent.

When the shaped carrier is present in a particular shape other than thehollow cylinders as defined, the crush strength or attrition resistancemay be measured by repeating the preparation of the shaped carrier withthe difference that the carrier is shaped into the hollow cylinders asdefined, instead of the particular shape, and the crush strength orattrition resistance of the hollow cylinders so obtained is measured.

Other than being as described above, the carriers that may be used inaccordance with this invention are not generally limited. Typically,suitable carriers comprise at least 85 percent by weight, more typically90 percent by weight, in particular 95 percent by weight alpha-alumina,frequently up to 99.9 percent by weight alpha-alumina, based on theweight of the carrier. The carrier may additionally comprise, silica,alkali metal, for example sodium and/or potassium, and/or alkaline earthmetal, for example calcium and/or magnesium.

Suitable carriers generally are also not limited with respect to surfacearea, water absorption, or other properties. However, it will beunderstood by those skilled in the art that surface area, waterabsorption, and other properties can affect the crush strength orattrition resistance of the carrier. The surface area of the carrier maysuitably be at least 0.1 m²/g, preferably at least 0.3 m²/g, morepreferably at least 0.5 m²/g, and in particular at least 0.6 m²/g,relative to the weight of the carrier; and the surface area may suitablybe at most 10 m²/g, preferably at most 5 m²/g, and in particular at most3 m²/g, relative to the weight of the carrier. “Surface area” as usedherein is understood to relate to the surface area as determined by theB.E.T. (Brunauer, Emmett and Teller) method as described in Journal ofthe American Chemical Society 60 (1938) pp. 309-316. High surface areacarriers, in particular when they are alpha-alumina carriers optionallycomprising in addition silica, alkali metal and/or alkaline earth metal,provide improved performance and stability of operation. However, whenthe surface area is very large, carriers tend to have lower crushstrength or attrition resistance.

The water absorption of the carrier may suitably be in the range of from0.2 to 0.8 g/g, preferably in the range of from 0.3 to 0.7 g/g, relativeto the weight of the carrier. A higher water absorption may be in favorin view of a more efficient deposition of silver and further elements,if any, on the carrier by impregnation. However, at higher waterabsorptions, the carrier, or the catalyst made therefrom, may have lowercrush strength or attrition resistance. As used herein, water absorptionis deemed to have been measured in accordance with ASTM C20, and waterabsorption is expressed as the weight of the water that can be absorbedinto the pores of the carrier, relative to the weight of the carrier.

Catalyst

In accordance with the present invention, the catalyst may comprise asilver component deposited on the previously described carrier havingincorporated therein a strength-enhancing amount of a strength-enhancingadditive.

The catalyst comprises silver as a catalytically active component.Appreciable catalytic activity is typically obtained by employing silverin an amount of at least 10 g/kg, calculated as the weight of theelement relative to the weight of the catalyst. Preferably, the catalystcomprises silver in a quantity of from 50 to 500 g/kg, more preferablyfrom 100 to 400 g/kg, for example 105 g/kg, or 120 g/kg, or 190 g/kg, or250 g/kg, or 350 g/kg.

The catalyst may comprise, in addition to silver, one or morehigh-selectivity dopants. Catalysts comprising a high-selectivity dopantare known from U.S. Pat. No. 4,761,394 and U.S. Pat. No. 4,766,105,which are incorporated herein by reference. The high-selectivity dopantsmay comprise, for example, components comprising one or more of rhenium,molybdenum, chromium, tungsten, and nitrate- or nitrite-formingcompounds. The high-selectivity dopants may each be present in aquantity of from 0.01 to 500 mmole/kg, calculated as the element (forexample, rhenium, molybdenum, tungsten, nitrogen, and/or chromium) onthe total catalyst. The nitrate- or nitrite-forming compounds andparticular selections of nitrate- or nitrite-forming compounds are asdefined hereinafter. The nitrate- or nitrite-forming compound is inparticular a Group IA metal nitrate or a Group IA metal nitrite.Rhenium, molybdenum, chromium, tungsten, or the nitrate- ornitrite-forming compound may suitably be provided as an oxide or as anoxyanion, for example, as a perrhenate, molybdate, tungstate, or nitratein salt or acid form. The high-selectivity dopants may be employed inthe preparation of the catalyst in a quantity sufficient to provide acatalyst having a content of high-selectivity dopant as disclosedherein.

Of special preference are catalysts that comprise a rhenium component,and more preferably also a rhenium co-promoter, in addition to silver.Rhenium co-promoters are selected from tungsten, molybdenum, chromium,sulfur, phosphorus, boron, compounds thereof, and mixtures thereof.

When the catalyst comprises a rhenium component, rhenium may typicallybe present in a quantity of at least 0.1 mmole/kg, more typically atleast 0.5 mmole/kg, and preferably at least 1 mmole/kg, in particular atleast 1.5 mmole/kg, calculated as the quantity of the element relativeto the weight of the catalyst. Rhenium is typically present in aquantity of at most 5 mmole/kg, preferably at most 3 mmole/kg, morepreferably at most 2 mmole/kg, in particular at most 1.5 mmole/kg.Again, the form in which rhenium is provided to the carrier is notmaterial to the invention. For example, rhenium may suitably be providedas an oxide or as an oxyanion, for example, as a rhenate or perrhenate,in salt or acid form.

If present, typical amounts of the rhenium co-promoter are from 0.1 to30 mmole/kg, based on the total amount of the relevant elements, i.e.,tungsten, molybdenum, chromium, sulfur, phosphorus and/or boron,relative to the weight of the catalyst. The form in which the rheniumco-promoter is provided to the carrier is not material to the invention.For example, the rhenium co-promoter may suitably be provided as anoxide or as an oxyanion, in salt or acid form.

Suitably, the catalyst may also comprise a Group IA metal component. TheGroup IA metal component typically comprises one or more of lithium,potassium, rubidium, and cesium. Preferably the Group IA metal componentis lithium, potassium and/or cesium. Most preferably, the Group IA metalcomponent comprises cesium or cesium in combination with lithium.Typically, the Group IA metal component is present in the catalyst in aquantity of from 0.01 to 100 mmole/kg, more typically from 0.50 to 50mmole/kg, more typically from 1 to 20 mmole/kg, calculated as the totalquantity of the element relative to the weight of the catalyst. The formin which the Group IA metal is provided to the carrier is not materialto the invention. For example, the Group IA metal may suitably beprovided as a hydroxide or salt.

As used herein, the quantity of Group IA metal present in the catalystis deemed to be the quantity in so far as it can be extracted from thecatalyst with de-ionized water at 100° C. The extraction method involvesextracting a 10-gram sample of the catalyst three times by heating it in20 mL portions of de-ionized water for 5 minutes at 100° C. anddetermining in the combined extracts the relevant metals by using aknown method, for example atomic absorption spectroscopy.

The preparation of the catalysts, including methods for incorporatingsilver, high-selectivity dopant, and Group IA metal is known in the artand the known methods are applicable to the preparation of the catalystthat may be used in accordance with the present invention. Methods ofpreparing the catalyst include impregnating the carrier with a silvercompound and performing a reduction to form metallic silver particles.Reference may be made, for example, to U.S. Pat. No. 5,380,697, U.S.Pat. No. 5,739,075, EP-A-266015, U.S. Pat. No. 6,368,998, WO-00/15333,WO-00/15334 and WO-00/15335, which are incorporated herein by reference.

The reduction of cationic silver to metallic silver may be accomplishedduring a step in which the catalyst is dried, so that the reduction assuch does not require a separate process step. This may be the case ifthe impregnation solution comprises a reducing agent, for example, anoxalate. Such a drying step is suitably carried out at a temperature ofat most 600° C., preferably at most 300° C., more preferably at most280° C., even more preferably at most 260° C., and suitably at atemperature of at least 100° C., preferably at least 200° C., morepreferably at least 210° C., even more preferably at least 220° C.,suitably for a period of time of at least 1 minute, preferably at least2 minutes, and suitably for a period of time of at most 60 minutes,preferably at most 20 minutes, more preferably at most 15 minutes, andmore preferably at most 10 minutes.

Epoxidation Process

Although the present epoxidation process may be carried out in manyways, it is desirable to carry it out as a gas phase process, i.e., aprocess in which the feed is contacted in the gas phase with thecatalyst which is present as a solid material, typically in a fixed bedunder epoxidation conditions. Epoxidation conditions are thosecombinations of conditions, notably temperature and pressure, underwhich epoxidation will occur. Generally the process is carried out as acontinuous process, such as the typical commercial process involvingfixed-bed, tubular reactors.

The typical commercial reactor has a plurality of elongated tubestypically situated parallel to each other. While the size and number oftubes may vary from reactor to reactor, a typical tube used in acommercial reactor will have a length between 4-15 meters and aninternal diameter between 1-7 centimeters. Suitably, the internaldiameter is sufficient to accommodate the catalyst. In particular, theinternal diameter of the tube is sufficient to accommodate the formedbodies of the carrier. Frequently, in commercial scale operation, theprocess of the invention may involve a quantity of catalyst which is atleast 10 kg, for example at least 20 kg, frequently in the range of from10² to 10⁷ kg, more frequently in the range of from 10³ to 10⁶ kg.

The olefin used in the present epoxidation process may be any olefin,such as an aromatic olefin, for example styrene, or a di-olefin, whetherconjugated or not, for example 1,9-decadiene or 1,3-butadiene. Mixturesof olefins may be used. Typically, the olefin is a mono-olefin, forexample 2-butene or isobutene. Preferably, the olefin is amono-α-olefin, for example 1-butene or propylene. The most preferredolefin is ethylene.

The olefin concentration in the feed may be selected within a widerange. Typically, the olefin concentration in the feed will be at most80 mole-%, relative to the total feed. Desirably, it will be in therange of from 0.5 to 70 mole-%, in particular from 1 to 60 mole-%, onthe same basis. As used herein, the feed is considered to be thecomposition that is contacted with the catalyst.

The present epoxidation process may be air-based or oxygen-based, see“Kirk-Othmer Encyclopedia of Chemical Technology”, 3^(rd) edition,Volume 9, 1980, pp. 445-447. In the air-based process, air or airenriched with oxygen is employed as the source of the oxidizing agentwhile in the oxygen-based processes high-purity (typically at least 95mole-%) oxygen is employed as the source of the oxidizing agent.Presently, most epoxidation plants are oxygen-based and this is apreferred embodiment of the present invention.

The oxygen concentration in the feed may be selected within a widerange. However, in practice, oxygen is generally applied at aconcentration that avoids the flammable regime. Typically, theconcentration of oxygen applied will be within the range of from 1 to 15mole-%, more typically from 2 to 12 mole-% of the total feed.

In order to remain outside the flammable regime, the concentration ofoxygen in the feed may be lowered as the concentration of the olefin isincreased. The actual safe operating ranges depend, along with the feedcomposition, on the reaction conditions such as the reaction temperatureand the pressure.

A reaction modifier may be present in the feed for increasing theselectivity, suppressing the undesirable oxidation of olefin or olefinoxide to carbon dioxide and water, relative to the desired formation ofolefin oxide. Many organic compounds, especially organic halides andorganic nitrogen compounds, may be employed as the reaction modifier.Nitrogen oxides, hydrazine, hydroxylamine or ammonia may be employed aswell. It is frequently considered that under the operating conditions ofolefin epoxidation the nitrogen containing reaction modifiers areprecursors of nitrates or nitrites, i.e. they are so-called nitrate- ornitrite-forming compounds (cf. e.g. EP-A-3642 and U.S. Pat. No.4,822,900, which are incorporated herein by reference).

Organic halides are the preferred reaction modifiers, in particularorganic bromides, and more in particular organic chlorides. Preferredorganic halides are chlorohydrocarbons or bromohydrocarbons. Morepreferably they are selected from the group of methyl chloride, ethylchloride, ethylene dichloride, ethylene dibromide, vinyl chloride or amixture thereof. Most preferred reaction modifiers are ethyl chlorideand ethylene dichloride.

Suitable nitrogen oxides are of the general formula NO_(x) wherein x isin the range of from 1 to 2, and include for example NO, N₂O₃ and N₂O₄.Suitable organic nitrogen compounds are nitro compounds, nitrosocompounds, amines, nitrates and nitrites, for example nitromethane,1-nitropropane or 2-nitropropane. In preferred embodiments, nitrate- ornitrite-forming compounds, e.g. nitrogen oxides and/or organic nitrogencompounds, are used together with an organic halide, in particular anorganic chloride.

The reaction modifiers are generally effective when used in lowconcentration in the feed, for example up to 0.1 mole-%, relative to thetotal feed, for example from 0.01×10⁻⁴ to 0.01 mole-%. In particularwhen the olefin is ethylene, it is preferred that the reaction modifieris present in the feed at a concentration of from 0.1×10⁻⁴ to 50×10⁻⁴mole-%, in particular from 0.3×10⁻⁴ to 30×10⁻⁴ mole-%, relative to thetotal feed.

In addition to the olefin, oxygen, and the reaction modifier, the feedmay contain one or more optional components, for example inert gases andsaturated hydrocarbons. Inert gases, for example nitrogen or argon, maybe present in the feed in a concentration of from 30 to 90 mole-%,typically from 40 to 80 mole-%, relative to the total feed. The feed maycontain saturated hydrocarbons. Suitable saturated hydrocarbons aremethane and ethane. If saturated hydrocarbons are present, they may bepresent in a quantity of up to 80 mole-%, relative to the total feed, inparticular up to 75 mole-%. Frequently they may be present in a quantityof at least 30 mole-%, more frequently at least 40 mole-%. Saturatedhydrocarbons may be added to the feed in order to increase the oxygenflammability limit.

The epoxidation process may be carried out using epoxidation conditions,including temperature and pressure, selected from a wide range.Preferably the reaction temperature is in the range of from 150 to 340°C., more preferably in the range of from 180 to 325° C. The reactiontemperature may be increased gradually or in a plurality of steps, forexample in steps of from 0.1 to 20° C., in particular 0.2 to 10° C.,more in particular 0.5 to 5° C. The total increase in the reactiontemperature may be in the range of from 10 to 140° C., more typicallyfrom 20 to 100° C. The reaction temperature may be increased typicallyfrom a level in the range of from 150 to 300° C., more typically from200 to 280° C., when a fresh catalyst is used, to a level in the rangeof from 230 to 340° C., more typically from 240 to 325° C., when thecatalyst has decreased in activity due to ageing.

The epoxidation process is typically carried out at a reactor inletpressure in the range of from 1,000 to 3,500 kPa. “GHSV” or Gas HourlySpace Velocity is the unit volume of gas at normal temperature andpressure (0° C., 1 atm, i.e., 101.3 kPa) passing over one unit volume ofpacked catalyst per hour. Preferably, when the epoxidation process is agas phase process involving a fixed catalyst bed, the GHSV is in therange of from 1500 to 10000 Nl/(l·h).

Carbon dioxide is a by-product in the epoxidation process, and thus maybe present in the feed. The carbon dioxide may be present in the feed asa result of being recovered from the product mix together withunconverted olefin and/or oxygen and recycled. Typically, aconcentration of carbon dioxide in the feed in excess of 25 mole-%,preferably in excess of 10 mole-%, relative to the total feed, isavoided.

An advantage of the present invention is that when the process isconducted at lower levels of carbon dioxide in the feed and the catalystcomprises a rhenium component, the process exhibits high peakselectivity and improved stability, including improved stability inselectivity and/or improved stability in activity. As such, the processof the present invention is desirably conducted under conditions wherethe concentration of carbon dioxide in the feed is lower than about 2mole-%, relative to the total feed. Suitably, a concentration of carbondioxide lower than about 1 mole-%, in particular lower than about 0.75mole-%, is used. Frequently, when practicing the present invention, theconcentration of carbon dioxide is at least 0.1 mole-%, and morefrequently the concentration of carbon dioxide is at least 0.3 mole-%. Aconcentration of carbon dioxide between about 0.50 mole-% and 0.75mole-% is particularly desirable. It is contemplated that the process ofthe present invention may be conducted at nominal concentrations ofcarbon dioxide in the feed, i.e., concentrations approaching if notreaching zero mole-%. Indeed, a process conducted in the absence ofcarbon dioxide in the feed is within the scope of the present invention.

Catalyst performance is conveniently measured using a standard set ofprocedures and process conditions. For example, a typical standardprocedure calls for 3.9 g of crushed catalyst to be loaded into astainless steel U-shaped tube. The tube is then immersed in a moltenmetal bath (heat medium) and the ends connected to a gas flow system.The weight of catalyst used and the inlet gas flow rate are adjusted togive a gas hourly space velocity of 3,300 Nl/(l·h), as calculated foruncrushed catalyst. The gas flow is then adjusted to 16.9 Nl/h with aninlet gas pressure of 1,370 kPa. The gas mixture passed through thecatalyst bed, in a “once-through” operation, during the entire test runincluding the start-up, is conveniently set at 30% v ethylene, 8% voxygen, 0.5% v carbon dioxide, 61.5% v nitrogen and 2.0 to 6.0 parts bymillion by volume (ppmv) ethyl chloride. The initial reactor temperatureis conveniently 180° C. and is ramped up at a rate of about 10° C. perhour to 225° C. and then adjusted so as to achieve a desired partialpressure of 41 kPa of ethylene oxide at the reactor outlet.

When operating at these operating conditions, the olefin epoxidationprocess using a catalyst comprising a silver component and a rheniumcomponent deposited on a fluoride-mineralized carrier, or carrier havinga particulate matrix having a lamellar or platelet-type morphology,having incorporated therein a strength-enhancing amount of astrength-enhancing additive, can achieve peak selectivities greater than85%. Preferably, the process achieves peak selectivities greater than87%. More preferably, the process achieves peak selectivities greaterthan 89% and even greater than 90%. Frequently, the process achievespeak selectivities of at most about 92%.

Additionally, when operating at these levels of carbon dioxide in thefeed, the olefin epoxidation process using a catalyst comprising asilver component and a rhenium component deposited on the carrier,having incorporated therein a strength-enhancing amount of astrength-enhancing additive, achieves improved stability.

The olefin oxide produced may be recovered from the product mix by usingmethods known in the art, for example by absorbing the olefin oxide froma product mix in water and optionally recovering the olefin oxide fromthe aqueous solution by distillation. At least a portion of the aqueoussolution containing the olefin oxide may be applied in a subsequentprocess for converting the olefin oxide into a 1,2-diol, a 1,2-diolether, or an alkanolamine. The methods employed for such conversions arenot limited, and those methods known in the art may be employed. Theterm “product mix” as used herein is understood to refer to the productrecovered from the outlet of the epoxidation reactor.

The conversion into the 1,2-diol or the 1,2-diol ether may comprise, forexample, reacting the olefin oxide with water, suitably using an acidicor a basic catalyst. For example, for making predominantly the 1,2-dioland less 1,2-diol ether, the olefin oxide may be reacted with a ten foldmolar excess of water, in a liquid phase reaction in the presence of anacid catalyst, e.g., 0.5-1.0% w sulfuric acid, based on the totalreaction mixture, at 50-70° C. at 1 bar absolute, or in a gas phasereaction at 130-240° C. and 20-40 bar absolute, preferably in theabsence of a catalyst. If the proportion of water is lowered theproportion of 1,2-diol ethers is increased. The 1,2-diol ethers thusproduced may be a di-ether, tri-ether, tetra-ether or a subsequentether. Alternatively, 1,2-diol ethers may be prepared by converting theolefin oxide with an alcohol, in particular a primary alcohol, such asmethanol or ethanol, by replacing at least a portion of the water by thealcohol.

The conversion into the alkanolamine may comprise reacting the olefinoxide with an amine, such as ammonia, an alkyl amine, or a dialkylamine.Anhydrous or aqueous ammonia may be used. Anhydrous ammonia is typicallyused to favor the production of monoalkanolamine. For methods applicablein the conversion of the olefin oxide into the alkanolamine, referencemay be made to, for example U.S. Pat. No. 4,845,296, which isincorporated herein by reference.

The 1,2-diol and the 1,2-diol ether may be used in a large variety ofindustrial applications, for example in the fields of food, beverages,tobacco, cosmetics, thermoplastic polymers, curable resin systems,detergents, heat transfer systems, etc. The alkanolamine may be used,for example, in the treating (“sweetening”) of natural gas.

Unless specified otherwise, the organic compounds mentioned herein, forexample the olefins, 1,2-diols, 1,2-diol ethers, alkanolamines, organicnitrogen compounds, and organic halides, have typically at most 40carbon atoms, more typically at most 20 carbon atoms, in particular atmost 10 carbon atoms, more in particular at most 6 carbon atoms. Asdefined herein, ranges for numbers of carbon atoms (i.e., carbon number)include the numbers specified for the limits of the ranges.

Having generally described the invention, a further understanding may beobtained by reference to the following example, which is provided forpurposes of illustration only and is not intended to be limiting unlessotherwise specified.

Example 1

A calcium acetate impregnating solution can be made by dissolving 28.28grams of calcium acetate in 165.0 grams of distilled water. 100 grams ofa gamma alumina cut into individual cylindrical formed bodies isevacuated to 20 mm Hg for 1 minute and the calcium acetate impregnatingsolution is then added to the gamma alumina while under vacuum. Thevacuum is then released and the transition alumina allowed to contactthe liquid for 3 minutes. The impregnated transition alumina would thenbe centrifuged at 500 rpm for 2 minutes to remove excess liquid. Thecalcium acetate impregnated transition alumina pellets is then dried inflowing nitrogen at 110° C. for 16 hours.

An ammonium fluoride impregnation solution can be made by dissolving19.965 grams of ammonium fluoride in 165 grams of distilled water.

The calcium acetate impregnated transition alumina can be evacuated to20 mm Hg for 1 minute and the ammonium fluoride impregnating solutioncan be added to the transition alumina while under vacuum. The vacuum isthen released and the transition alumina allowed to contact the liquidfor 3 minutes. The impregnated transition alumina is then centrifuged at500 rpm for 2 minutes to remove excess liquid. Impregnated transitionalumina pellets are then dried in flowing nitrogen at 120° C. for 16hours.

The dried impregnated transition alumina is then placed in a first hightemperature alumina crucible. Approximately 50 g of calcium oxide isplaced in a second high temperature alumina crucible. The hightemperature alumina crucible containing the impregnated transitionalumina is placed into the second high temperature alumina crucible,which contains the calcium oxide, and is then covered with a third hightemperature alumina crucible of smaller diameter than the secondcrucible, such that the impregnated transition alumina is locked in bythe third crucible and the calcium oxide. This assembly is then placedinto a furnace at room temperature. The temperature of the furnace isincreased from room temperature to 800° C. over a period of 30 minutes.The assembly is then held at 800° C. for 30 minutes and thereafterheated to 1,200° C. over a period of 1 hour. The assembly is then heldat 1,200° C. for 1 hour. The furnace is then allowed to cool and thealumina is removed from the assembly.

The resultant carrier can then be tested for crush strength or attritionresistance using respectively ASTM D6175-03 or ASTM D4058-96, asdescribed herein, or some other methods for measuring crush strength orattrition resistance. The results can be compared to those of differentcarriers prepared using different amounts of calcium acetate, differentstrength-enhancing additives, or no strength-enhancing additives. Thus,a carrier having incorporated therein a strength-enhancing amount of astrength-enhancing additive can be obtained. This carrier can then beused to prepare an olefin epoxidation catalyst, which can then be usedin a process for the production of an olefin oxide, and subsequently a1,2-diol, a 1,2-diol ether or an alkanolamine.

We claim:
 1. A process for preparing a catalyst for the epoxidation ofan olefin comprising: incorporating a strength-enhancing additive into acarrier which has a particulate matrix having a lamellar orplatelet-type morphology; calcining the carrier at a temperature in therange of from greater than 900° C. to less than 1200° C.; andsubsequently depositing a catalytic species onto the carrier wherein thestrength-enhancing additive comprises a lanthanide Group species.
 2. Theprocess as claimed in claim 1, wherein the lamellar or platelet-typemorphology is such that particles having in at least one direction asize greater than 0.1 micrometer have at least one substantially flatmajor surface.
 3. The process as claimed in claim 1, wherein thestrength-enhancing additive comprises cerium.
 4. The process as claimedin claim 1, wherein the carrier comprises alpha-alumina.
 5. The processas claimed in claim 1, wherein the catalytic species comprises one ormore of silver, molybdenum, nickel, and tungsten.
 6. The process asclaimed in claim 5, wherein the catalytic species comprises silver. 7.The process as claimed in claim 6, wherein the process additionallycomprises depositing a high selectivity dopant onto the carrier.
 8. Theprocess as claimed in claim 6, wherein the process additionallycomprises depositing a Group IA metal component onto the carrier.
 9. Theprocess as claimed in claim 7, wherein the process additionallycomprises depositing a rhenium component, or a rhenium component and arhenium co-promoter onto the carrier.
 10. The process as claimed inclaim 1 further comprising: subsequently heating the carrier and thecatalytic species deposited thereon at a temperature in the range offrom 100° C. to 600° C.